• Proceedings of the Materials Research Society of Korea Conference
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• 2003.03a
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• pp.227-227
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• 2003

흑연(graphite), 석탄(coal), 숯(char), soot(검댕이) 등의 탄소로 이루어진 재료들은 비정질부터 완전한 흑연결정까지 다양한 구조를 나타낸다. 이러한 탄소재료의 구조의 출발물질 뿐 아니라 열처리에 따라 강한 영향을 받는다 이러한 구조는 여러 구조인자에 의해 특성화되는데, 구조인자로는 층간거리 d, 결정립 크기 Lc 그리고 결정립 직경 La이다. 이런 구조 인자의 지식은 흑연화, 탄소화, 가스화 등과 같은 다양한 공정을 이해하는데 매우 중요하다. 많은 연구자들은 XRD, Raman 분광, 고분해능 TEM 등과 같은 여러 기술을 통하여 이러한 구조인자에 대한 해석을 시도하였다. 그 중 XRD는 정량적 분석에 있어서 가장 많이 이용되는 기술이다. XRD 회절피크의 위치로부터 층간거리 d를 구할 수 있으며, 결정립 크기 Lc 및 결정립 직경 La는 피크의 line 퍼짐(반가폭)으로 직접 구할 수 있다. 한편 섬유상 흡착제로 이용되는 등방성 탄소섬유는 이산화탄소 또는 수증기에 의해 쉽게 활성화되어 최고 약 2,500 $m^2$/g의 고 비 표면적을 얻을 수 있다. 이렇게 활성화 후 고 비표면적을 나타내는 이유는 좁은 분포를 나타내는 미세기공의 기공구조 때문에 발생하는 것으로 알려져 있다.

• Journal of Energy Engineering
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• v.25 no.3
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• pp.9-17
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• 2016

In this study, a method for CO reduction using char-coal combustions was developed with lignin and glycerin as combustion improvers. The relationship between CO emission and the combustion improvers was confirmed by measuring the CO concentration. The experiment to determine the combustion characteristics was conducted using glycerin, which shows high combustibility at low temperatures, impregnated with lignin, which has a specific surface area. The combustibility, volatility, and CO concentration were measured using thermo-gravimetric analysis(TGA), and gas chromatography-mass spectrometry(GC-MS). This study presents the optimal CO reduction ratio, which occurred when the combustible material contained a 20% blend of combustion improvers. This resulted in a 20-30% CO reduction rate compared to that achieved with normal char-coal.

• Clean Technology
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• v.2 no.1
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• pp.60-68
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• 1996

The oxidation of carbon monoxide of low concentration on the natural manganese dioxide (NMD) has been investigated in a fixed bed reactor. The experimental variables were concentration of oxygen (500ppm~99.8%) and carbon monoxide (500ppm~10000ppm) and catalyst temperature ($50{\sim}750^{\circ}C$). The NMD(Natural Manganese Dioxide) has been characterized by temperature - program reduction(TPR) using 2.4% $CO/H_2$ as a reducing agent, thermogravimetric analysis (TGA), and reduction of NMD by 2.4% $CO/H_2$. It was found that the NMD catalyst activity on the unit area was greater than the $MnO_2$ catalyst for oxidation of CO at the same temperature. The thermal stability of oxidation activity was considered to be maintained when the NMD was heated to $750^{\circ}C$. The TGA, reduction by CO, and TPR of the NMD showed that the NMD had active lattice oxygen which was easily liberated on heating in the absence and low concentration of oxygen. The reaction order in CO is 0.701 between 500~3500ppm and almost zero between 3500~10000ppm of CO.

• Journal of the Korea institute for structural maintenance and inspection
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• v.25 no.5
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• pp.165-172
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• 2021

The purpose of this study is to investigate the carbon capture capacity of various inorganic materials. For this purpose, the change in property of ordinary Portland cement (OPC), blast furnace slag fine powder (GGBS), and circulating fluidized bed boiler ash (CFBC) due to carbonation were analyzed. Carbonation curing was performed on all specimens through the accelerated carbonation experiment, and the amount of carbon capture was quantitatively analyzed by thermogravimetric analysis according to the age of carbonation. From the results, it is confirmed that the carbon capture capacity was shown in all specimens. The carbon capture amount was shown in the order of CFBC, OPC, and GGBS. The 28-day carbon capture of CFBC, OPC, and GGBS was 3.9%, 1.3%, and 9.4%, respectively. Carbon capture reaction occurred rapidly at the beginning of carbonation, and occurred slowly with increasing age. SEM image analysis revealed that an additional product generated by carbonation curing in all specimens was calcium carbonate.

• Proceedings of the Korean Institute of Industrial Safety Conference
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• 2002.11a
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• pp.301-304
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• 2002

화재대피용 방독마스크의 주요한 기능은 상온에서의 일산화탄소 제거이며, 가장 효과적인 방법은 촉매에 의한 것이다. 일산화탄소 제거를 위한 호흡용 보호구의 정화통 충진재로써 범용으로 쓰이는 촉매는 Hopcalite로 Cu와 Mn이 혼합된 산화물 촉매이다. 그러나 이들 촉매는 상온에서 CO의 제거효율이 낮아 많은 양을 충진해야 하는 어려움이있다.(중략)

• Proceedings of the Korean Vacuum Society Conference
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• 2015.08a
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• pp.141.1-141.1
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• 2015

탄소나노튜브는 우수한 전기적 특성과 더불어 열전도도, 강도, 높은 화학적 안정성, 바이오 물질과의 친화성 때문에 많은 응용이 가능하며 최근까지도 활발히 연구되는 대표적인 탄소질의 물질이다. 이러한 다중 벽 탄소나노튜브를 제품화시키기 위해서는 특정 용매에서 용이한 분산성을 지닐 수 있도록 기능화 공정이 필수적이고 많은 양의 파우더를 기능화 시킬 수 있는 장비의 구조 및 공정개선이 요구된다. 플라즈마 기술을 이용한 건식의 순환형 나노분산 파우더 플라즈마 반복처리장치를 통하여 기능화 처리된 탄소나노튜브를 습식공정에 비해 간편한 공정으로 재현성 있고 균일한 결과로 많은 양의 확보가 가능하다. 이에 탄소나노튜브의 기능화 결과를 제시함으로써 본 장비를 소개하고자 한다.

• Applied Chemistry for Engineering
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• v.26 no.1
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• pp.92-98
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• 2015

In this study, phenol-based activated carbons (ACs) were fluorinated at various fluorine partial pressures (0.01~0.03 MPa) and the $Cr^{6+}$ ion adsorption of fluorinated ACs was investigated. According to BET and XPS results, the specific surface area and total pore volume of fluorinated ACs increased by 24.7 and 55.8%, respectively, and fluorine functional groups were introduced to AC surface. The most optimized condition of $Cr^{6+}$ ion adsorption was confirmed at the fluorine partial pressure of 0.02 MPa. And also the removal efficiency of $Cr^{6+}$ ion was up to 98% at 300 mg/L of the initial concentration, and these results showed an approximately three-fold increase compared to that of using untreated ACs. Furthermore, the $Cr^{6+}$ ion adsorption of fluorinated ACs was completed in less than 30 min in contrast with untreated ACs, which was expected to be an increase of the affinity between $Cr^{6+}$ ions and ACs surfaces by fluorination.

• Applied Chemistry for Engineering
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• v.5 no.2
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• pp.189-198
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• 1994

The adsorptive behaviors of carbon monoxide and methanol over $V_2O_5$catalyst were studied by means of thermal desorptlon spectroscopy (TDS) under ultrahigh vacuum conditions. Carbon monoxide adsorbed on oxygen-deficient V sites as well as on V=O groups of the $V_2O_5$ surface. CO adsorbed on the V sites desorbed at 380 K while CO adsorbed on the V=O groups formed carbonate species with surface oxygen of $V_2O_5$ and desorbed as $CO_2$ resulting in the reduction of the surface of she $V_2O_5$catalyst. The amount of CO adsorbed in the form of carbonate species increased by both the pre- and post-adsorbed oxygen. The adsorptive behavior of methanol over the catalyst was studied by thermal desorption experiments of $CH_3OH$, HCHO, CO, and $H_2$ upon methanol adsorption at 298 K. The results showed that methanol was adsorbed dissociatively on the $V_2O_5$catalyst as methoxy and hydroxyl groups at 298K.

• Journal of the Korean Chemical Society
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• v.54 no.3
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• pp.323-328
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• 2010

In this work, an intention to synthesize the carbon molecular sieve (CMS) with ideal sieving properties from palm shell has been attempted. The process includes three main stages: carbonization, carbon dioxide activation and polymer deposition using polyfurfuryl alcohols. Palm shell based activated carbon (AC) produced by carbon dioxide activation was used as raw material in synthesis of CMS. After preparing palm shell based AC, optimum concentration ratio of furfuryl alcohols and formaldehyde to AC for CMS synthesis was obtained in this study. Deposition of polyfurfuryl alcohols on the palm shell based AC was then carried out prior to carbonization. These polymer deposited AC was subjected to carbonization at $700-900^{\circ}C$ under inert condition. All the microporous materials were analyzed using micromeritics ASAP/2020. The results show that optimum concentration ratio of furfuryl alcohol and formaldehyde to AC is 1:2.5. The micropore with pore width less than 7 ${\AA}$ was formed on the polymer deposited AC at $700^{\circ}C$, $800^{\circ}C$ and $900^{\circ}C$ for 1.5 hours. Carbonization temperature at $900^{\circ}C$ for 1.5 hours was found to be optimum for CMS synthesis. The CMS produced under this condition has pore width of 5.884 ${\AA}$.

• Applied Chemistry for Engineering
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• v.26 no.3
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• pp.239-246
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• 2015

The hybridization of carbon nano-materials enhances the efficiency of each function of the resulting structure or composites. Also, the addition of non-carbon elements to nanomaterials modifies the electrochemical properties. Electrodes combining porous carbon nanofibers (CNFs) and metal oxides benefit from the combination of the double-layer capacitance of the CNFs and the pseudocapacitive character associated with the surface redox-type reactions. Consequently, they demonstrate superior supercapacitor performance in terms of high capacitance, high energy/power efficiency and high rate capability. This paper presents a comprehensive review of the latest advances made in the development and application of various metal oxide/CNF composites (CNFCs) to supercapacitor electrodes.